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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353195Generated: October 30, 2026

Sodium Bicarbonate → tert-Butyl 2-methyl-2-[4-({[(4-methyl-1,3-oxazol-5-yl)methyl]amino}methyl)-phenoxy]-propanoate

https://huagongshe.com/reaction/353195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl 2-(4-formylphenoxy)-2-methylpropanoateHCID 22708193—
Reactant(4-Methyl-1,3-oxazol-5-yl)methylamineHCID 22708194—
Solvent1,2-DichloroethaneHCID 11—
Producttert-Butyl 2-methyl-2-[4-({[(4-methyl-1,3-oxazol-5-yl)methyl]amino}methyl)-phenoxy]-propanoateHCID 22708253—

Reaction Steps

1.25 g (4.73 mmol) of tert-butyl 2-(4-formylphenoxy)-2-methylpropanoate (Example I-4) and 0.64 g (5.67 mmol) of (4-methyl-1,3-oxazol-5-yl)methylamine (Example III-28) are together initially charged in 1,2-dichloroethane. At room temperature, 1.50 g (7.09 mmol) of sodium triacetoxyborohydride are added. The reaction mixture is stirred at room temperature for 4 hours and then admixed with saturated sodium bicarbonate solution and extracted with ethyl acetate. The organic phase is dried over magnesium sulphate and freed from the solvent under reduced pressure. The residue is purified chromatographically on silica gel (dichloromethane/methanol 30:1) and then dried under reduced pressure. This gives 1.104 g (65% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06750236B2
Source datasetuspto-grants-2004_06
ORD IDord-15aa678edc724d93a93c78d1067b1645
Source noteuspto-grants-2004_06